Publications:

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HaploCoV: unsupervised classification and rapid detection of novel emerging variants of SARS-CoV-2.

Communications Biology

Chiara, Matteo M; Horner, David S DS; Ferrandi, Erika E; Gissi, Carmela C; Pesole, Graziano G

Publication Date: 2023-04-22

Variant appearance in text: GC: 785T>C

PubMed Link: 37087497

Variant Present in the following documents:

• 42003_2023_4784_MOESM4_ESM.xlsx, sheet 1

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A Novel High-Content Phenotypic Screen To Identify Inhibitors of Mitochondrial DNA Maintenance in Trypanosomes.

Antimicrobial Agents And Chemotherapy

Miskinyte, Migla M; Dawson, John C JC; Makda, Ashraff A; Doughty-Shenton, Dahlia D; Carragher, Neil O NO; Schnaufer, Achim A

Publication Date: 2022-02-15

Variant appearance in text: GC: L262P

PubMed Link: 34871097

Variant Present in the following documents:

• aac.01980-21.pdf

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Glanzmann Thrombasthenia: Perspectives from Clinical Practice on Accurate Diagnosis and Optimal Treatment Strategies.

Journal Of Blood Medicine

Mathews, Natalie N; Rivard, Georges-Etienne GE; Bonnefoy, Arnaud A

Publication Date: 2021

Variant appearance in text: GC: Leu262Pro

PubMed Link: 34149292

Variant Present in the following documents:

• jbm-12-449.pdf

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Intratumoral heterogeneity as a predictive biomarker in anti-PD-(L)1 therapies for non-small cell lung cancer.

Molecular Cancer

Fang, Wenfeng W; Jin, Haoxuan H; Zhou, Huaqiang H; Hong, Shaodong S; Ma, Yuxiang Y; Zhang, Yaxiong Y; Su, Xiaofan X; Chen, Longyun L; Yang, Yunpeng Y; Xu, Shengqiang S; Liao, Yuwei Y; He, Yuming Y; Zhao, Hongyun H; Huang, Yan Y; Gao, Zhibo Z; Zhang, Li L

Publication Date: 2021-02-23

Variant appearance in text: GC: 785T>C; Leu262Ser

PubMed Link: 33622313

Variant Present in the following documents:

• 12943_2021_1331_MOESM3_ESM.xlsx, sheet 4

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Redesigned and reversed: architectural and functional oddities of the trypanosomal ATP synthase.

Parasitology

Gahura, Ondřej O; Hierro-Yap, Carolina C; Zíková, Alena A

Publication Date: 2021-09

Variant appearance in text: GC: L262P

PubMed Link: 33551002

Variant Present in the following documents:

• S0031182021000202a.pdf

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Accessing unexplored regions of sequence space in directed enzyme evolution via insertion/deletion mutagenesis.

Nature Communications

Emond, Stephane S; Petek, Maya M; Kay, Emily J EJ; Heames, Brennen B; Devenish, Sean R A SRA; Tokuriki, Nobuhiko N; Hollfelder, Florian F

Publication Date: 2020-07-10

Variant appearance in text: GC: L262P

PubMed Link: 32651386

Variant Present in the following documents:

• 41467_2020_17061_MOESM2_ESM.pdf

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NOTCH target gene HES5 mediates oncogenic and tumor suppressive functions in hepatocarcinogenesis.

Oncogene

Luiken, Sarah S; Fraas, Angelika A; Bieg, Matthias M; Sugiyanto, Raisatun R; Goeppert, Benjamin B; Singer, Stephan S; Ploeger, Carolin C; Warsow, Gregor G; Marquardt, Jens U JU; Sticht, Carsten C; De La Torre, Carolina C; Pusch, Stefan S; Mehrabi, Arianeb A; Gretz, Norbert N; Schlesner, Matthias M; Eils, Roland R; Schirmacher, Peter P; Longerich, Thomas T; Roessler, Stephanie S

Publication Date: 2020-04

Variant appearance in text: GC: 785T>C

PubMed Link: 32055024

Variant Present in the following documents:

• 41388_2020_1198_MOESM2_ESM.xlsx, sheet 1

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Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study.

Orphanet Journal Of Rare Diseases

Sánchez-Guiu, Isabel I; Antón, Ana I AI; Padilla, José J; Velasco, Francisco F; Lucia, José F JF; Lozano, Miguel M; Cid, Ana Rosa AR; Sevivas, Teresa T; Lopez-Fernandez, María F MF; Vicente, Vicente V; González-Manchón, Consuelo C; Rivera, José J; Lozano, María L ML

Publication Date: 2014-12-24

Variant appearance in text: GC: Leu262Pro

PubMed Link: 25539746

Variant Present in the following documents:

• 13023_2014_Article_213.pdf

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High-resolution transcriptome analysis with long-read RNA sequencing.

Plos One

Cho, Hyunghoon H; Davis, Joe J; Li, Xin X; Smith, Kevin S KS; Battle, Alexis A; Montgomery, Stephen B SB

Publication Date: 2014

Variant appearance in text: GC: L262P

PubMed Link: 25251678

Variant Present in the following documents:

• pone.0108095.pdf

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